ExomeDepth (1.1.10)

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Calls Copy Number Variants from Targeted Sequence Data.


Calls copy number variants (CNVs) from targeted sequence data, typically exome sequencing experiments designed to identify the genetic basis of Mendelian disorders.

Maintainer: Vincent Plagnol
Author(s): Vincent Plagnol

License: GPL-3

Uses: aod, VGAM, knitr

Released over 1 year ago.

6 previous versions



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